Health product recall

Azurion R3.0 Systems

Last updated

Summary

Product
Azurion R3.0 Systems
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

Azurion 7 M20

Not applicable.

722234

Azurion 5 M12

Not applicable.

722231

Azurion 7 M12

Not applicable.

722233

Azurion 3 M12

Not applicable.

722229

Azurion 3 M15

Not applicable.

722230

Azurion 7 B12

Not applicable.

722235

Azurion 7 B20

Not applicable.

722236

Azurion 5 M20

Not applicable.

722232

Issue

Philips has identified nine software issues affecting Azurion R3.0 systems that may result in loss of imaging (X-ray) functionality, and/or loss of motorized movement, and/or incorrect image content, and/or loss of data.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies

Philips Medical Systems Nederland B.V.

Veenpluis 6, Best, Netherlands, 5684 PC

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-81381

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